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Common breast cancer susceptibility alleles are associated with tumour subtypes in BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of B... von Mulligan, Anna Marie, Couch, Fergus J, Barrowdale, Daniel, Domchek, Susan M, Eccles, Diana, Nevanlinna, Heli, Ramus, Susan J, Robson, Mark, Sherman, Mark, Spurdle, Amanda B, Wappenschmidt, Barbara, Lee, Andrew, McGuffog, Lesley, Healey, Sue, Sinilnikova, Olga M, Janavicius, Ramunas, Hansen, Thomas vO, Nielsen, Finn C, Ejlertsen, Bent, Osorio, Ana, Muñoz-Repeto, Iván, Durán, Mercedes, Godino, Javier, Pertesi, Maroulio, Benítez, Javier, Peterlongo, Paolo, Manoukian, Siranoush, Peissel, Bernard, Zaffaroni, Daniela, Cattaneo, Elisa, Bonanni, Bernardo, Viel, Alessandra, Pasini, Barbara, Papi, Laura, Ottini, Laura, Savarese, Antonella, Bernard, Loris, Radice, Paolo, Hamann, Ute, Verheus, Martijn, Meijers-Heijboer, Hanne E J, Wijnen, Juul, Gómez García, Encarna B, Nelen, Marcel R, Kets, C Marleen, Seynaeve, Caroline, Tilanus-Linthorst, Madeleine M A, van der Luijt, Rob B, van Os, Theo, Rookus, Matti, Frost, Debra, Jones, J Louise, Evans, D Gareth, Lalloo, Fiona, Eeles, Ros, Izatt, Louise, Adlard, Julian, Davidson, Rosemarie, Cook, Jackie, Donaldson, Alan, Dorkins, Huw, Gregory, Helen, Eason, Jacqueline, Houghton, Catherine, Barwell, Julian, Side, Lucy E, McCann, Emma, Murray, Alex, Peock, Susan, Godwin, Andrew K, Schmutzler, Rita K, Rhiem, Kerstin, Engel, Christoph, Meindl, Alfons, Ruehl, Ina, Arnold, Norbert, Niederacher, Dieter, Sutter, Christian, Deissler, Helmut, Gadzicki, Dorothea, Kast, Karin, Preisler-Adams, Sabine, Varon-Mateeva, Raymonda, Schoenbuchner, Ines, Fiebig, Britta, Heinritz, Wolfram, Schäfer, Dieter, Gevensleben, Heidrun, Caux-Moncoutier, Virginie, Fassy-Colcombet, Marion, Cornelis, François, Mazoyer, Sylvie, Léoné, Mélanie, Boutry-Kryza, Nadia, Hardouin, Agnès, Berthet, Pascaline, Muller, Danièle, Fricker, Jean-Pierre, Mortemousque, Isabelle, Pujol, Pascal
Veröffentlicht in Breast cancer research : BCR
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Common Variants at the 19p13.1 and ZNF365 Loci Are Associated with ER Subtypes of Breast Cancer and Ovarian Cancer Risk in BRCA1 and BRCA2 Mutation Carriers von COUCH, Fergus J, GAUDET, Mia M, MCGUFFOG, Lesley, BARROWDALE, Daniel, LEE, Andrew, HEALEY, Sue, SINILNIKOVA, Olga M, ANDRULIS, Irene L, OZCELIK, Hilmi, MULLIGAN, Anna Marie, THOMASSEN, Mads, GERDES, Anne-Marie, ANTONIOU, Antonis C, BIRK JENSEN, Uffe, SKYTTE, Anne-Bine, KRUSE, Torben A, CALIGO, Maria A, VON WACHENFELDT, Anna, BARBANY-BUSTINZA, Gisela, LOMAN, Niklas, SOLLER, Maria, EHRENCRONA, Hans, KARLSSON, Per, RAMUS, Susan J, NATHANSON, Katherine L, REBBECK, Timothy R, DOMCHEK, Susan M, JAKUBOWSKA, Ania, LUBINSKI, Jan, JAWORSKA, Katarzyna, DURDA, Katarzyna, ZLOWOCKA, Elzbieta, HUZARSKI, Tomasz, BYRSKI, Tomasz, KUCHENBAECKER, Karoline B, GRONWALD, Jacek, CYBULSKI, Cezary, GORSKI, Bohdan, OSORIO, Ana, DURAN, Mercedes, ISABEL TEJADA, Maria, BENITEZ, Javier, HAMANN, Ute, HOGERVORST, Frans B. L, OS, Theo A. Van, SOUCY, Penny, LEEUWEN, Flora E. Van, MEIJERS-HEIJBOER, Hanne E. J, WIJNEN, Juul, BLOK, Marinus J, KETS, Marleen, HOONING, Maartje J, OLDENBURG, Rogier A, AUSEMS, Margreet G. E. M, PEOCK, Susan, BEESLEY, Jonathan, XIAOQING CHEN, XIANSHU WANG, KIRCHHOFF, Tomas
Veröffentlicht in Cancer epidemiology, biomarkers & prevention
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Ovarian cancer susceptibility alleles and risk of ovarian cancer in BRCA1 and BRCA2 mutation carriers von Ramus, Susan J., Kuchenbaecker, Karoline B., Beesley, Jonathan, Healey, Sue, Thomassen, Mads, Jensen, Uffe Birk, Skytte, Anne-Bine, Lindblom, Annika, Olsson, Håkan, Melin, Beatrice, Domchek, Susan M., Nathanson, Katherine L., Jakubowska, Anna, Lubinski, Jan, Jaworska, Katarzyna, Durda, Katarzyna, Złowocka, Elżbieta, Gronwald, Jacek, Huzarski, Tomasz, Byrski, Tomasz, Benitez, Javier, Tejada, Maria-Isabel, Aalfs, Cora M., Meijers-Heijboer, Hanne E.J., van Asperen, Christi J., van Roozendaal, K.E.P., Collée, J. Margriet, van der Luijt, Rob B., Frost, Debra, Platte, Radka, Fineberg, Elena, Evans, D. Gareth, Lalloo, Fiona, Jacobs, Chris, Adlard, Julian, Davidson, Rosemarie, Cook, Jackie, Paterson, Joan, Morrison, Patrick J., Kennedy, M. John, Godwin, Andrew K., Caux-Moncoutier, Virginie, Gauthier-Villars, Marion, Mazoyer, Sylvie, Lasset, Christine, Hardouin, Agnès, Berthet, Pascaline, Faivre, Laurence, Buys, Saundra, Beth Terry, Mary, Chung, Wendy K., John, Esther M, Tea, Muy-Kheng, Pfeiler, Georg, Fink-Retter, Anneliese, Hansen, Thomas v. O., Ejlertsen, Bent, Offit, Kenneth, Gaudet, Mia M., Vijai, Joseph, Robson, Mark, Phillips, Kelly-Anne, Hoffman, James S, Montagna, Marco, Tognazzo, Silvia, Isaacs, Claudine, Janavicius, Ramunas, Blanco, Ignacio, Navarro, Matilde, Karlan, Beth Y., Olah, Edith, Vaszko, Tibor, Teo, Soo-Hwang, Ganz, Patricia A., Diez, Orland, Schmutzler, Rita K., Wappenschmidt, Barbara, Engel, Christoph, Meindl, Alfons, Arnold, Norbert, Niederacher, Dieter, Deissler, Helmut, Fiebig, Britta, Nevanlinna, Heli, Aittomäki, Kristiina, Plante, Marie, Spurdle, Amanda B., Ding, Yuan Chun, Lindor, Noralane, Fredericksen, Zachary, Pankratz, V. Shane, Peissel, Bernard, Bernard, Loris, Dolcetti, Riccardo, Radice, Paolo, Greene, Mark H., Mai, Phuong L., Ozcelik, Hilmi, Couch, Fergus J., Chenevix-Trench, Georgia
Veröffentlicht in Human mutation
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Haplotype structure in Ashkenazi Jewish BRCA1 and BRCA2 mutation carriers von Im, Kate M., Kirchhoff, Tomas, Wang, Xianshu, Green, Todd, Chow, Clement Y., Korn, Joshua, Gaudet, Mia M., Fredericksen, Zachary, Shane Pankratz, V., Guiducci, Candace, Crenshaw, Andrew, McGuffog, Lesley, Kartsonaki, Christiana, Morrison, Jonathan, Healey, Sue, Sinilnikova, Olga M., Mai, Phuong L., Greene, Mark H., Piedmonte, Marion, Rubinstein, Wendy S., Hogervorst, Frans B., Rookus, Matti A., Collée, J. Margriet, Hoogerbrugge, Nicoline, Meijers-Heijboer, Hanne E. J., Van Roozendaal, Cees E., Perez-Segura, Pedro, Jakubowska, Anna, Huzarski, Tomasz, Blecharz, Paweł, Nevanlinna, Heli, Aittomäki, Kristiina, Lazaro, Conxi, Blanco, Ignacio, Barkardottir, Rosa B., D’Andrea, Emma, Devilee, Peter, Olopade, Olufunmilayo I., Peissel, Bernard, Bonanni, Bernardo, Peterlongo, Paolo, Singer, Christian F., Rennert, Gad, Lejbkowicz, Flavio, Andrulis, Irene L., Ozcelik, Hilmi, Toland, Amanda Ewart, Caligo, Maria Adelaide, Beattie, Mary S., Chan, Salina, Domchek, Susan M., Nathanson, Katherine L., Rebbeck, Timothy R., Phelan, Catherine, Narod, Steven, John, Esther M., Hopper, John L., Buys, Saundra S., Southey, Melissa C., Terry, Mary-Beth, Tung, Nadine, Hansen, Thomas v. O., Benitez, Javier, Weitzel, Jeffrey N., Garber, Judy, Hamann, Ute, Peock, Susan, Cook, Margaret, Oliver, Clare T., Frost, Debra, Eeles, Ros, Izatt, Louise, Paterson, Joan, Brewer, Carole, Hodgson, Shirley, Porteous, Mary, Walker, Lisa, Rogers, Mark T., Side, Lucy E., Godwin, Andrew K., Wappenschmidt, Barbara, Laitman, Yael, Deissler, Helmut, Varon-Mateeva, Raymonda, Preisler-Adams, Sabine, Kast, Karin, Venat-Bouvet, Laurence, Stoppa-Lyonnet, Dominique, Chenevix-Trench, Georgia, Easton, Douglas F., Klein, Robert J., Daly, Mark J., Friedman, Eitan, Dean, Michael, Clark, Andrew G., Altshuler, David M., Antoniou, Antonis C., Couch, Fergus J., Offit, Kenneth, Gold, Bert
Veröffentlicht in HUMAN GENETICS
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Stroke genetics informs drug discovery and risk prediction across ancestries von Kamanu, F.K., Koido, M., Caro, I., Lin, K., Winsvold, B.S., Parodi, L., Tomppo, L., Jee, Y.H., Abedi, V., Lewis, A.J., Ago, T., Amouyel, P., Bis, J.C., Bordes, C., Borte, S., Cain, A., Cruchaga, C., Cole, J.W., Cid, R. de, Endres, M., Gudnason, V., Havulinna, A.S., Hyacinth, H.I., Jacob, M.A., Jeon, C.E., Jern, C., Kamouchi, M., Keene, K.L., Kittner, S.J., Kumar, A., Launer, L.J., Lee, K.J., Li, L.M., Manichaikul, A., Markus, H.S., Meitinger, T., Nalls, M.A., Nordestgaard, B.G., Onland-Moret, N.C., Peters, A., Sacco, R.L., Saleheen, D., Sandset, E.C., Salomaa, V., Sasaki, M., Schmidt, C.O., Smith, N.L., Tiedt, S., Vugt, M. van, Verma, S.S., Wiggins, K.L., Woo, D., Wilson, P.W.F., Xu, H.C., Yang, Q., Yoon, K., Meschia, J.F., Traylor, M., Carty, C.L., Reiner, A., Gottesman, R.F., Furie, K.L., Arnett, D.K., Benavente, O.R., Grewal, R.P., Peddareddygari, L.R., Lindstrom, S., Smith, E.N., Vlieg, A.V., Brody, J.A., Pattee, J.W., Giulianini, F., Ibrahim, M., McCauley, B.M., Kraft, P., Hansen, J.B., Morange, P.E., Kabrhel, C., Dijk, E.J. van, Luijckx, G.J., Oostenbrugge, R.J. van, Wermer, M.J.H., Leeuw, F.E. de, Levi, C.R., Ilinca, A., Rothwell, P.M., Butterworth, A.S., Rolfs, A., Weir, D., Jood, K., Linkohr, B., Lee, T.H., Anderson, C.D., Jian, X.Q., Schminke, U., Ibanez, L., Muino, E., Roquer, J., Sarnowski, C., Kanai, M.
Veröffentlicht in Nature
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Identification of a BRCA2-Specific Modifier Locus at 6p24 Related to Breast Cancer Risk von Gaudet, M.M, Klein, R.J, Kirchhoff, T, McGuffog, L, Dunning, A.M, Lee, A, Dennis, J, Healey, S, Dicks, E, Sinilnikova, O, Pankratz, V.S, Wang, X, Eldridge, R.C, Tessier, D.C, Bacot, F, Hogervorst, F.B.L, Peock, S, Stoppa-Lyonnet, D, Peterlongo, P, Schmutzler, R.K, Nathanson, K.L, Piedmonte, M, Singer, C.F, Hansen, T.V.O, Neuhausen, S.L, Garber, J, Weitzel, J.N, Andrulis, I.L, Goldgar, D.E, D'Andrea, E, Caldes, T, Nevanlinna, H, Osorio, A, van Rensburg, E.J, Arason, A, van den Ouweland, A.M.W, van der Hout, A.H, Kets, C.M, Wijnen, J.T, Ausems, M.G.E.M, Frost, D, Platte, R, Evans, D.G, Jacobs, C, Tischkowitz, M, Damiola, F, Golmard, L, Barjhoux, L, Belotti, M, Ferrer, S.F, Spurdle, A.B, Manoukian, S, Genuardi, M, Arnold, N, Sutter, C, Wappenschmidt, B, Pfeiler, G, Friedman, E, Jensen, U.B, Robson, M, Shah, S, Mai, P.L, Fasching, P.A, Peto, J, Humphreys, M.K, Michailidou, K, Sawyer, E.J, Burwinkel, B, Guenel, P, Milne, R.L, Brenner, H, Lochmann, M, Aittomaki, K, Doerk, T, Margolin, S, Mannermaa, A, Lambrechts, D, Chang-Claude, J, Radice, P, Giles, G.G, Winqvist, R, Garcia-Closas, M, Schoof, N, Hooning, M.J, Cox, A, Jakubowska, A, Orr, N, Pita, G, Rosario Alonso, M, Hall, P, Couch, F.J, Simard, J, Altshuler, D, Chenevix-Trench, G, Antoniou, A.C, Offit, K, HEBON, EMBRACE, Collaborators, GEMOS, Network, GENICA
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